Canonical Allele Identifier: CA413606186
Community Standard Title: NM_000052.7(ATP7A):c.4328C>G (p.Thr1443Ser)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046395C>G , CM000685.2:g.78046395C>G GRCh38
NC_000023.10:g.77301892C>G , CM000685.1:g.77301892C>G GRCh37
NC_000023.9:g.77188548C>G NCBI36
NG_013224.2:g.140699C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4328C>G (ATP7A) MANE Select NP_000043.4:p.Thr1443Ser
ENST00000341514.11:c.4328C>G (ATP7A) MANE Select ENSP00000345728.6:p.Thr1443Ser
NM_000052.6:c.4328C>G (ATP7A) NP_000043.4:p.Thr1443Ser
NM_001282224.1:c.4094C>G (ATP7A) NP_001269153.1:p.Thr1365Ser
NM_001282224.2:c.4094C>G (ATP7A) NP_001269153.1:p.Thr1365Ser
NR_104109.1:n.1538C>G (ATP7A)
NR_104109.2:n.1501C>G (ATP7A)
ENST00000341514.10:c.4328C>G (ATP7A) ENSP00000345728.6:p.Thr1443Ser
ENST00000343533.10:c.4358C>G (ATP7A) ENSP00000343026.6:p.Thr1453Ser
ENST00000343533.9:c.4094C>G (ATP7A) ENSP00000343026.5:p.Thr1365Ser
ENST00000350425.5:c.*3501C>G (ATP7A) ENSP00000343678.5:n.*3501C>G
ENST00000644362.1:c.-19-63472C>G (PGK1) ENSP00000496140.1:n.-19-63472C>G
ENST00000682475.1:n.2745C>G (ATP7A)
ENST00000685033.1:c.1592C>G (ATP7A) ENSP00000509269.1:p.Thr531Ser
ENST00000685264.1:c.4328C>G (ATP7A) ENSP00000510136.1:p.Thr1443Ser
ENST00000686033.1:c.4133C>G (ATP7A) ENSP00000510693.1:p.Thr1378Ser
ENST00000686133.1:c.4328C>G (ATP7A) ENSP00000509233.1:p.Thr1443Ser
ENST00000686255.1:n.3359C>G (ATP7A)
ENST00000686543.1:c.4094C>G (ATP7A) ENSP00000509477.1:p.Thr1365Ser
ENST00000687086.1:c.4328C>G (ATP7A) ENSP00000509566.1:p.Thr1443Ser
ENST00000689083.1:n.1623C>G (ATP7A)
ENST00000689767.1:c.4421C>G (ATP7A) ENSP00000509406.1:p.Thr1474Ser
ENST00000692908.1:c.4094C>G (ATP7A) ENSP00000508627.1:p.Thr1365Ser